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The nucleolar protein nucleophosmin is essential for autophagy induced by inhibiting Pol I transcription.


ABSTRACT: Various cellular stresses activate autophagy, which is involved in lysosomal degradation of cytoplasmic materials for maintaining nutrient homeostasis and eliminating harmful components. Here, we show that RNA polymerase I (Pol I) transcription inhibition induces nucleolar disruption and autophagy. Treatment with autophagy inhibitors or siRNA specific for autophagy-related (ATG) proteins inhibited autophagy but not nucleolar disruption induced by Pol I transcription inhibition, which suggested that nucleolar disruption was upstream of autophagy. Furthermore, treatment with siRNA specific for nucleolar protein nucleophosmin (NPM) inhibited this type of autophagy. This showed that NPM was involved in autophagy when the nucleolus was disrupted by Pol I inhibition. In contrast, NPM was not required for canonical autophagy induced by nutrient starvation, as it was not accompanied by nucleolar disruption. Thus, our results revealed that, in addition to canonical autophagy, there may be NPM-dependent autophagy associated with nucleolar disruption.

SUBMITTER: Katagiri N 

PROVIDER: S-EPMC4354046 | biostudies-literature | 2015 Mar

REPOSITORIES: biostudies-literature

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The nucleolar protein nucleophosmin is essential for autophagy induced by inhibiting Pol I transcription.

Katagiri Naohiro N   Kuroda Takao T   Kishimoto Hiroyuki H   Hayashi Yuki Y   Kumazawa Takuya T   Kimura Keiji K  

Scientific reports 20150310


Various cellular stresses activate autophagy, which is involved in lysosomal degradation of cytoplasmic materials for maintaining nutrient homeostasis and eliminating harmful components. Here, we show that RNA polymerase I (Pol I) transcription inhibition induces nucleolar disruption and autophagy. Treatment with autophagy inhibitors or siRNA specific for autophagy-related (ATG) proteins inhibited autophagy but not nucleolar disruption induced by Pol I transcription inhibition, which suggested t  ...[more]

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